NDC 30805-007 Symmetry Non-alcohol Foaming Hand Sanitizer

NDC Product Code 30805-007

NDC 30805-007-02

Package Description: 1250 mL in 1 BAG

NDC 30805-007-07

Package Description: 550 mL in 1 BOTTLE, PUMP

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Symmetry Non-alcohol Foaming Hand Sanitizer with NDC 30805-007 is a product labeled by Buckeye International, Inc.. The generic name of Symmetry Non-alcohol Foaming Hand Sanitizer is . The product's dosage form is and is administered via form.

Labeler Name: Buckeye International, Inc.

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • ALLANTOIN (UNII: 344S277G0Z)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
  • LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
  • EDETATE SODIUM (UNII: MP1J8420LU)
  • METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Buckeye International, Inc.
Labeler Code: 30805
Start Marketing Date: 06-09-2009 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2018 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Symmetry Non-alcohol Foaming Hand Sanitizer Product Label Images

Symmetry Non-alcohol Foaming Hand Sanitizer Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Active ingredientBenzalkonium Chloride 0.24%

Indications & Usage

UsesHand sanitizer to help reduce bacteria on the skin that could cause diseaseRecommended for repeated use

Warnings

WarningsFor external use only

Otc - When Using

When using this product do not use in or near eyes.If in eyes, flush thoroughly with water.

Adverse Reactions

If irritation or rash appears and persists, stop use and see a physician.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, call a physician or Poison Control Center immediately.

Dosage & Administration

DirectionsDispense an adequate amount of hand sanitizerRub hands together until completely dry

Inactive Ingredient

Inactive ingredientsWater (Aqua), Cocamidopropyl Betaine, Lauramine Oxide, Tetrasodium EDTA, Allantoin, Fragrance (Parfum), Aloe Barbadensis Leaf Juice, Methylchloroisothiazolinone, Methylisothiazolinone

Otc - Questions

Questions?Call: Buckeye International, Inc. 314-291-1900Monday through Friday 8:00 to 5:00 p.m. CST

Otc - Purpose

PurposeAntibacterial

* Please review the disclaimer below.